Position-independent and tissue specific expression of a transgene in milk of transgenic animals

ABSTRACT

The present invention relates to an isolated insulator DNA molecule consisting of the 5′ and 3′ regions of the porcine wrap gene locus and a method for insulating the expression of an introduced heterologous gene from silencing and variegation effect in chromatin into which the gene has integrated. The invention is also directed to mammalian cells comprising said insulator DNA molecule and non human animals obtained therefrom, which are preferably able to express a polypeptide of interest in milk.

SEQUENCE LISTING

The instant application contains a “Sequence Listing” which has been submitted via duplicate CD-R, and is hereby incorporated by reference in its entirety. The CD-Rs are labeled “CRF” and “Copy 1,” respectively, and each contains only one identical 317 kb file, created Jun. 29, 2004. The data contained in the duplicate CD-R “Sequence Listing” are identical to the data contained in the paper “Sequence Listing,” submitted Apr. 6, 2004.

The present invention relates to an isolated insulator DNA molecule consisting of the 5′ and 3′ regions of the porcine wap gene locus and a method for insulating the expression of an introduced heterologous gene from silencing and variegation effect in chromatin into which the gene has integrated. The invention is also directed to mammalian cells comprising said insulator DNA molecule and non human animals obtained therefrom, which are preferably able to express a polypeptide of interest in milk.

The milk is one of the biological fluid which is considered as a major potential source of recombinant proteins for pharmaceutical use and human consumption. The microinjection of hybrid gene containing a promoter specific of the mammary gland into fertilized oocytes has been successfully done since 1987. A general review on transgenic animals as bioreactors and methods for obtaining transgenic animals is available in Houdebine (2000).

However, the proteins encoded by the transgenes may have deleterious effects on transgenic animal health when they are not specifically expressed in the mammary gland of lactating animals. In the other hand, the yield of foreign proteins in the milk of transgenic animals is not predictable and often low. Moreover, the level of expression varies among lines (Palmiter et al., 1984) and even sometimes among animals of the same line (Al-Shawi et al., 1988; Dobie et al., 1996). This fact is dependent mainly of the various integration sites of the transgene into the host genome. Consequently, it often occurs a silencing of the transgenes and variegation providing a mosaicism of transgene expression into tissues from a same animal (Dobie et al., 1997; Festenstein et al., 1996 and Alami et al., 2000).

Different approaches have been proposed to improve the expression of gene constructs. First, some cis-regulatory elements can be linked to the transgene and thus suppress the position effect. For example, the locus control regions (LCR) from the human β-globin cluster or from the CD2 gene are able to confer a position-independent, copy-dependent and tissue-specific expression even if the transgene is integrated near the centromere (Festenstein et al., 1996; Milot et al., 1996). Moreover, insulator elements like the 5′end of the chicken β-globin locus (Chung et al., 1993; Taboit-Dameron et al., 1999), the region spanning the DNase I hypersensitive site (HS) 2-6 of the human T cell receptor (Zhong and Krangel, 1999) or an Alu element from the keratin-18 gene (Willoughby et al., 2000) are able to confer position-independent expression in transgenic mice. For a review of such elements see also U.S. Pat. No. 6,100,448 (increasing expression of transgenes in plant cells using insulator elements), U.S. Pat. No. 6,037,525, (method for reducing expression variability of transgenes in plant cells), and U.S. Pat. No. 5,610,053 (DNA sequence which acts as a chromatin insulator element to protect expressed genes from cis-acting regulatory sequences in mammalian cells). The second possibility is to use long genomic fragments expected to contain all the elements sufficient for an appropriate expression of the transgene. Indeed, the correct expression of the human ApoB gene was obtained in the liver and intestine of transgenic mice after microinjection of a large genomic DNA fragment (70 kb downstream and 22 kb upstream the ApoB gene) but not with smaller fragments (19 kb downstream and 17.5 kb upstream the ApoB gene) (Nielsen et al., 1997).

So far, a few milk protein genes have been expressed in a position-independent fashion in transgenic animals. This was the case for the sheep β-lactoglobulin gene (Whitelaw et al., 1992), the rat WAP gene (Krnacik et al., 1995), the goat α-lactalbumin gene in a BAC vector (Stinnakre et al., 1999) and the human α-lactalbumin gene in a YAC vector (Fujiwara et al., 1997). However, the unpredictability of the expression pattern of most of the transgenes, attributed to the various integration sites of the transgene into the host genome, impedes the preparation of animals that efficiently express transgenes of interest in milk.

The present invention solves the above mentioned problems in that it provides insulator elements allowing position-independent expression of transgenes.

Another issue is to ensure an efficient production of transgenes of interest in milk. Whey acidic protein (WAP) is the major whey protein of rodents (Campbell et al., 1984; Hennighausen and Sippel, 1982), rabbit (Devinoy et al., 1988; Grabowski et al., 1991) and camel (Beg et al., 1986). It has been identified in pig milk (Simpson et al., 1998). The wap gene promoter from mouse or rabbit have been used to direct the production of recombinant proteins in the mammary gland of transgenic animals. The upstream region of mouse wap gene associated to the human protein C (hPC) gene allowed the production of 0.1 to 1.8 g/l of the hPC in the milk of transgenic swine (Van Cott et al., 1996). The bovine growth hormone gene controlled by a 6.3 kb upstream fragment of the rabbit wap gene was expressed at 1 to 16 g/l level in the milk (Thépot et al., 1995). However, these levels varied among lines regardless of the integrated copy numbers and the specificity of expression was dependent on the integration site.

The invention further provides with cis-regulatory elements which are able to direct the efficient expression of the transgene of interest in milk, leading to production of large quantities of heterologous proteins.

In this regard, we have cloned the pig wap cDNA and prepared BAC constructs containing the entire porcine wap gene. The comparison of the coding sequence of the pig wap gene to rodent or lagomorph wap sequence known in the art demonstrated that only exon sequences are partially conserved.

The porcine wap gene was localized on the subtelomeric region of the chromosome 18. The estimation of the expression of the swine wap gene in the mammary gland from lactating animals revealed a high level of expression. In order to compare the expression level of the porcine wap gene from the large genomic fragment which contained 70 kb downstream and 50 kb upstream the pig wap gene or the smaller one (1 kb downstream and 2.4 kb upstream), these two genomic fragments were transfected in HC11 cell line. The BAC construct was expressed fifteen times higher than the plasmid when reported to the integrated copy number. Thus, we demonstrated that the mouse mammary epithelial HCl 11 cell line is useful as a tool to identify the regulatory sequences of milk protein genes.

Then, we showed using HCl 11 cells, that one of theses BAC clones, which has 70 kb upstream and 50 kb downstream the wap gene, allowed an expression fifteen times higher than a fragment containing 1 kb of the upstream region.

The expression specificity of a transgene containing the porcine wap gene surrounding with 140 kb upstream region and 5 kb downstream region was tested. Level of expressions was compared between the different transgenic mouse line and the endogenous expression in the mammary gland of a lactating swine.

Thus, the invention provides long genomic fragments isolated around the porcine wap gene which contain all of the regulatory elements necessary to optimize gene expression of a transgene in milk of transgenic animals. Such sequences contain both cis-regulatory elements and insulators allowing position-independent and efficient tissue specific expression of transgenes in milk.

Description

The present invention is aimed at an isolated insulator DNA molecule consisting of the 5′ and 3′ regions of the porcine wap gene locus, wherein said DNA molecule is isolated from a NotI-NotI fragment of about 145 kb and 75 kb obtainable from BAC 905F9 or BAC 344H5 deposited on Dec. 13, 2000 at the Collection Nationale de Cultures de Micro-organismes (CNCM), Institut Pasteur, 28, rue du Dr Roux, 75724 Paris cédex 15, under the accession numbers I-2595 and I-2596 respectively.

The entire genomic sequence of the porcine wap gene from 40 nucleotides upstream and 2047 downstream the cap site is depicted as SEQ ID No1.

The term “insulator” refers to a DNA segment that prevent the influence of elements in the surrounding chromatin, which act on promoters to enhance or silence gene expression; V. Corces, Nature 376, 462 (Aug. 10, 1995). Where two insulators are employed, they may be the same or different. The insulator according to the invention may encompass fragments of the naturally occurring insulator isolated from the wap gene locus, so long as it retains function as an insulator. The length of the insulator is not critical, but may generally be from 100, 200, or 300 bases up 2000, 3000, 5000, 10000 or more bases in length. In connection with the invention, longer fragments may be used so as to incorporate the cis-acting elements of the wap gene locus and therefore allow efficient expression of heterologous proteins in milk of transgenic animals.

Thus, the DNA molecule according to the invention can further comprise the cis-acting regulatory sequences of the porcine wap gene. The cis-acting regulatory sequences are enhancers that can form a “milk box” and correspond to binding sequences of transcription factors such as GRE, MAF or Stat-5, MPBF, C/EBP and YYI or other factors.

In a second embodiment, the invention is directed to a vector comprising:

-   (a) at least one isolated insulator DNA molecule as described above; -   (b) a promoter domain; -   (c) a heterologous gene operably linked to the promoter domain.

In such a vector, at least one (1, 2, or more) insulator is positioned 5′ of the promoter so as to operably insulate the transcription and expression of the gene from cis-acting regulatory elements in chromatin into which the gene has integrated.

Alternatively, at least one insulator is positioned 3′ of the gene so as to operably insulate the transcription and expression of the gene from cis-acting regulatory elements in chromatin into which the gene has integrated. A vector in which the heterologous gene to be expressed in framed between two insulators is also contemplated.

The term “operatively associated,” as used herein, refers to DNA sequences on a single DNA molecule which are associated so that the function of one is affected by the other. Thus, a transcription initiation region is operatively associated with a structural gene when it is capable of affecting the expression of said structural gene.

Vectors according to the invention can be retroviral vectors selected from the spumaviruses; the lentiviruses and the oncoviruses.

Retroviruses are enveloped single-stranded RNA viruses which infect animal cells. When a retrovirus infects a cell, its RNA genome is converted into a double-stranded linear DNA form, which is integrated into the host cell genome. Viral vectors, including recombinant retroviral vectors, provide a more efficient means of transferring genes into cells as compared to other techniques such as calcium phosphate-DNA co-precipitation or DEAE-dextran-mediated transfection, electro-poration, microinjection or lipofection of nucleic acids.

A third embodiment of the invention relates to a DNA construct comprising an expression cassette, which construct comprises, in the 5′ to 3′ direction, a transcription initiation region, a structural gene positioned downstream from said transcription initiation region and operatively associated therewith, and an insulator according to one of claims 1 to 3 positioned 5′ to the transcription initiation region and/or 3′ to the structural gene. Such DNA construct can take the form of a vector as mentioned above but also of a plasmid, naked-DNA, episomal vector or artificial chromosome. It is also possible to provide two distinct constructs, one comprising an insulator DNA sequence according to the invention and the other comprising the heterologous gene to be expressed, both construct being injected together in an host cell.

Advantageously, constructs mentioned above can be microinjected directly into early embryos, ES cells, totipotent cells and oocytes, or introduced in spermatic cells.

Among the preferred embodiments, a DNA construct or a vector as depicted above wherein said promoter is the rabbit wap gene promoter allowing efficient expression of a structural gene in milk of animals is contemplated (the rabbit wap gene promoter is described in U.S. Pat. No. 5,965,788). Of course, any other constitutive, or tissue-specific promoter may be employed in frame with the invention.

Among structural genes that can be employed are those encoding a polypeptide or protein selected from antibodies, growth factors, polypeptide, blood factors, enzymes or peptide as commodities or of therapeutic value.

A DNA construct or a vector as depicted above comprising the sequence SEQ ID No1 is also contemplated.

Another embodiment of the invention relates to a method for insulating the expression of an introduced heterologous gene from silencing and variegation effect in chromatin into which the gene has integrated, comprising:

-   (a) providing a vector or a DNA construct as mentioned above; -   (b) transfecting a mammalian cell with said vector or DNA construct;     and -   (c) integrating the vector or the DNA construct into the chromatin     of said cell,     wherein the expression of a resultant integrated gene is insulated     from cis-acting DNA regulatory sequences in the chromatin of said     cell.

In a particular embodiment, the invention concerns a method for insulating the expression of an introduced heterologous gene from silencing comprising:

-   (a) providing an episomal vector as mentioned above; -   (b) transfecting a mammalian cell with said vector.

The invention also relates to a method of making transgenic non-human animals having increased expression of an heterologous gene, said method comprising:

-   a) transforming a mammalian cell with a vector or a DNA construct as     mentioned above; -   b) and generating non-human animals from said cell.

A preferred mammalian cell may be an oocyte which has not undergone the final stages of gametogenesis and which can be infected with the herein retroviral vector.

The injected oocytes are then permitted to complete maturation with the accompanying meiotic divisions. The breakdown of the nuclear envelope during meiosis permits the integration of the proviral form of the retrovirus vector into the genome of the oocyte. The injected oocytes can be cultured in vitro under conditions which permit maturation prior to fertilization in vitro. Conditions for the maturation of oocytes from a number of mammalian species (e.g., bovine, ovine, porcine, murine, caprine) are well known to the art. One can refer for example to U.S. Pat. No. 6,080,912 (methods for creating transgenic animals) and to U.S. Pat. No. 5,994,619 (production of chimeric bovine or porcine animals using cultured inner cell mass cells).

Oocytes may also be matured in vivo to practice the present invention. Retroviral vectors capable of infecting the desired species of non-human animals which can be grown and concentrated to very high may be employed as mentioned above. The use of high titer virus stocks allows the introduction of a defined number of viral particles into the perivitelline space of each injected oocyte. In vitro culture conditions which permit the maturation of pre-maturation oocytes from a variety of mammalian species (e.g., cattle, hamster, pigs and goats) are well know to the art [see Parrish et al. (1985) Theriogenology 24:537; Rosenkrans and First (1994) J. Ani. Sci. 72:434; Bavister and Yanagimachi (1977) Biol. Reprod. 16:228; Bavister et al. (1983) Biol. Reprod. 28:235; Leibfried and Bavister (1982) J. Reprod. Fert. 66:87; Keskintepe et al. (1994) Zygote 2:97 Funahashi et al. (1994) J. Reprod. Fert. 101:159 and Funahashi et al. (1994) Biol. Reprod 50:1072].

Other cells that are very useful for obtaining transgenic animals, except humans, are totipotent, pluripotent and ES cells. Methods for culturing and transforming such cells are described in WO 00/27995 (ES cells), WO 00/15764 (propagation and derivation of ES cells), WO 99/27076 (pluripotent embryonic stem cells and methods of obtaining them), WO 99/10488 (site-specific recombination in eukaryotes and constructs useful therefor), U.S. Pat. No. 5,690,926 (pluripotential embryonic cells and methods of making same), WO 97/41209 (pluripotent rabbit embryonic stem cell lines and use in the generation of chimeric rabbit), WO 97/20035 (establishement, maintenance and transfection of totipotent embryonic stem cells from the embryos of animals), U.S. Pat. No. 5,166,065 (in vitro propagation of embryonic stem cells), WO 95/20042 (ES cells isolation), WO 94/23049 (the introduction and expression of large genomic sequences in transgenic animals), WO 99/09141 (porcine totipotent cells and method for long-term culture), WO 97/49803 (trangenesis by genetic transfer into one blastomere of an embryo), WO 97/20035 (establishment, maintenance and transfection of totipotent ES cells from embryos of domestic animals), WO 96/07732 (Totipotent cells for nuclear transfer) and AU3395695 (totipotent cells for nuclear transfer).

Therefore, the invention is also aimed at a mammalian cell, notably at a mammalian cell selected from oocytes, totipotent, pluripotent and ES cells, wherein a DNA construct or a vector as described above has integrated the chromatin of said cells.

According to the state of the art, it is now possible to produce a transformed a somatic cell such as a fibroblast with a vector or a DNA construct according to the invention and to use it for the nuclear transfer into a recipient cell which will in turn produce an embryo. Nuclear transfer techniques are described in WO 95/17500, WO 97/07668, WO 97/07669, WO 98/30683, WO 99/01163 and WO 99/37143.

As a result, another embodiment is directed to a transgenic non-human animal having increased expression of an heterologous gene comprising a cell according to the invention.

Such animals can be selected for example from the group consisting of cows, pigs, sheep, goats, rabbits, rats, and mice.

The invention is not limited to the embodiments depicted above and contemplates as well the following:

The invention also concerns the use of an isolated insulator DNA described herein for preventing the silencing and variegation effect of chromatin into which a heterologous gene has integrated.

For example, it is possible to practice the invention for insulating the differential expression of two genes, consisting of a providing:

-   (a) at least one isolated insulator molecules according to the     invention; -   (b) a first expressible gene; (c) a second expressible gene; (d) a     promoter that mediates expression of said first gene operably linked     to said first gene; (e) a promoter that mediates expression of said     second gene operably linked to said second gene; -   (f) an enhancer operably linked to the second gene so as to enhance     expression of said second gene,     wherein said one or more of the insulators is positioned in the     construct 5′ of the promoter operably linked to the first gene;     wherein the enhancer is positioned 5′ of the promoter operably     linked to the second gene which is positioned in opposite     transcriptional orientation to said first gene; and further wherein     one or more of the insulators is positioned 3′ of the first and     second genes.

Alternatively, it is provided a DNA construct for insulating the differential expression of two genes encoding two different proteins comprising:

-   (a) one or more isolated eukaryotic insulator molecules according to     any of claim 2, or 3; (b) a first expressible gene; (c) a second     expressible gene; (d) a promoter that mediates expression of said     first second gene operably linked to the first gene; (e) a promoter     that mediates expression of said second gene operably linked to the     second gene; (f) a first enhancer operably linked to the first gene     so as to enhance expression of said first gene; and (g) a second     enhancer operably linked to the second gene so as to enhance     expression of said second gene;     wherein one or more of the insulators is positioned between the     first and second enhancer; wherein the first enhancer is operable to     enhance the transcriptional activity of the promoter of the first     gene; and wherein the second enhancer is operable to enhance the     transcriptional activity of the promoter of the second gene; and     further wherein one or more of the insulators is positioned at the     3′ of the first and second genes.

Another possibility to practice the invention is to use an isolated insulator DNA described herein for preventing the silencing and variegation effect of chromatin into which two heterologous genes have been integrated. Indeed, it is possible to direct the simultaneous expression of two different structural genes, wherein at least one Internal Ribosome Entry Site is operatively linked to at least one of said genes.

A general review of IRES controlled translation is available in Houdebine et Attal, 1999, Transgenic research, 8: 157-177 and in Ohlmann et al, January 2000, m/s (medecines/sciences), vol 16, 77-86. More specifically, retroviral vectors containing IRES and methods of gene transfer using retrotransposons have been described in WO 93/03143 and WO 92/07950, respectively. Different DNA constructs for expressing simultaneously two genes in a vector comprising a promoter and an IRES is depicted at FIG. 1 of WO 96/01324.

The wap gene has exons with large percentage of identity with rodent and rabbit wap gene. Introns are less conserved as judged by sequence homology and size. Moreover, some of the common transcription signals are also conserved. Indeed, the potential TATA box is a modified TATA consensus sequence like in other WAP gene and the polyadenylation signals is identical.

In order to determine if the cis-regulatory elements of the porcine wap gene may be interesting to direct production of recombinant protein in the mammary gland, an evaluation of the expression of the endogenous wap gene in pig was necessary. First, we determine if the level of expression of the porcine wap gene was comparable to the expression of the rabbit and mouse wap gene. We chose to evaluate the mRNA concentration at the beginning of lactation. It was easy to detect endogenous wap mRNA from the three species since only thirty minutes of exposition were required to reveal intense signals. The pig wap mRNA seemed to be slightly less abundant than those of the mouse and rabbit. Since the mouse and the rabbit wap gene are abundantly expressed in the mammary gland of lactating animals, the pig wap gene seemed also to be well expressed in the mammary gland of lactating swine.

In order to determine if the expression was more intense with large fragment of genomic DNA, porcine wap gene associated to only 1 kb of the promoter region (pWAPpXhoI) and one of the BAC clones which contained 70 kb upstream and 50 kb downstream of the porcine wap gene (BAC 905F9) were transfected in epithelial cell from mammary mouse (HC11). A lower number of the integrated copies was detected from cells transfected by the BAC clone than with the smaller genomic fragment. It may be explained by the size difference between the BAC clone (150 kb) and the plasmid (8,5 kb). Indeed, a DNA fragment 16 times lower than an other one may have more opportunities to be integrated in the host genome. This expression was not detectable by Northern blot analysis and a RT-PCR was performed to compare the two expressions. It was then demonstrated that the BAC 905F9 clone was expressed fifteen times higher than in the smaller genomic fragment when reported to copy number. This may be explained by the presence of additional enhancers and insulators in the long genomic fragment. Moreover, the expression of the wap gene from the BAC clones seemed to be more sensitive to lactogenic hormones since the level of expression increased gradually with insulin, insulin and prolactin, insulin and corticoids and the three hormones (data not shown). These results concur to the evidence that the genomic fragment contain the distal regulatory sequences of milk protein genes. However, only transgenic animals are expected to indicate if this BAC clone is able to give a specific and high expression in the mammary gland of lactating animals (see below).

In order to produce porcine WAP protein in the milk of transgenic mice, a 150 kb DNA fragment from a bacterial artificial chromosome insert containing the porcine WAP-encoding transcription unit was purified according to two different techniques. The first involved a simple phenol-chloroform extraction whereas the other used the GELase enzyme and a dialysis. Both were equally efficient to generate mouse transgenic lines. It then appeared that the usual phenol-chloroform technique may be used to prepare long DNA fragment for microinjection into mouse fertilized oocytes. However, the disadvantage of this method is that the DNA fragment harboring the gene of interest is not separated from the others. The remaining prokaryotic DNA may disturb transgene expression by favoring the methylation of the exogenous DNA or by interfering with the normal environment of the transgene. Interestingly, this fact was not observed. This result confirms that the long DNA fragment harboring the pig wap gene also contained insulators.

Eight animals were transgenic. Two were obtained with phenol-chloroform purified DNA and six with DNA prepared with the other method. One animal did never transmit its transgene and an other one died before he could reproduce. Six lines were then analyzed. All the lactating animals from these lines expressed the porcine wap gene in the mammary gland. Hence, the long genomic fragment allowed expression to be independent of the integration site.

Furthermore, this expression was detected only in the mammary gland. In a virgin animal, no porcine wap mRNA and no endogenous mouse wap mRNA were found by Northern blotting. The expression was therefore developmentally regulated. This DNA fragment thus contains the cis-acting elements involved in the control of the porcine wap gene expression.

The examination of mouse milk composition confirmed this conclusion. A protein expected to be pig WAP was detected by Coomassie brilliant blue coloration only in the milk and in the whey of animals from the line 16. Here, it is shown that the animal BAC16 expressed strongly the porcine wap gene since the corresponding recombinant protein was at a level higher than this of the endogenous murine protein and was more than ten times more concentrated than in the porcine whey. The concentration of the murine WAP protein is known to reach approximately 3 to 5 mg/ml (Hennighausen and Sippel, 1982). The porcine WAP protein was present at this level if not more in the milk of the animal BAC16.

It is further shown that the expression level correlates with the number of integrated copies. The line 16 which harbors 26 copies of the transgene has an expression level 8 fold higher than that of the line 28 which has only 3 copies. However, no difference in the level of expression can be shown clearly in animals harboring only one or two copies since the variation between lines was roughly equal to the differences between animals within the same line.

The porcine BAC clone containing the wap gene according to the invention is therefore able to direct transgene expression in the lactating mammary gland irrespectively of the integration site. So far, only a few milk protein genes have been expressed in a position-independent fashion in transgenic mice. This was the case for the sheep β-lactoglobulin gene (Whitelaw et al., 1992), the rat wap gene (Kmacik et al., 1995), the human α-lactalbumin gene in a YAC (Fujiwara et al., 1997) and the goat α-lactalbumin gene in a BAC (Stinnakre et al., 1999). The porcine BAC clone of the invention represents a new tool to tightly control expression of recombinant protein encoding genes in the mammary gland of lactating transgenic animals. In conclusion, the data here demonstrates that the BAC construct harboring the porcine wap gene contains cis-regulatory elements as well as insulators.

LEGENDS

FIG. 1: Partial map of the WAPpXhoI insert (A) and partial enzyme distribution over the two more interesting BAC clones containing the porcine WAP gene (B). (▪) indicates the location of the four exons of the porcine WAP gene. (□) indicates the location of the entire porcine WAP gene. A: AscI; X: XhoI; E: EcORI; N: NotI.

FIG. 2: wap gene transcription in mammary gland of lactating swine, rabbit and mouse. Total RNA (10 and 20 μg) from mammary gland of five days lactating swine and from mammary gland of three days lactating rabbit and mouse were fractionated on denaturing 1.5% agarose/formaldehyde gels, blotted and hybridized to the mouse (A), swine (B) and rabbit (C) wap cDNA labeled by ³²P-dCTP. The equal loading of RNA sample is shown by UV/Ethidium bromide picture of 28 and 18S rRNA (D).

FIG. 3: Porcine wap gene expression in mouse epithelial cell line (HC11). HC11 cell line was cotransfected with the RSVneo and pWAPpXhoI or BAC 905F9. Pools of clones were selected by G418 (150 μg/ml). Cells were cultured as described in. Materials and Methods and harvested 48 h after the hormonal treatment (Insulin, Dexamethasone, Prolactine). A: Specific porcine wap RT-PCR was performed on non transfected HC11 cell line (NT), pWAPpXhoI pool (pWAPpXhoI) and BAC905F9 pool (BAC905). PCR products were electrophosed on 2% agarose gel. B:PCR products were blotted on nylon membrane and hybridized with labelled porcine cDNA wap1.4 probe. C: To normalize PCR amplification, the endogenous mouse GAPDH cDNA was amplified from RT products, electrophosed on 2% agarose gel, blotted and hybridized with the labelled mouse GAPDH cDNA probe.

D: The number of integrated copies were evaluated by Southern blot using 10 μg of genomic DNA from non transfected HC11 cells (NT), pWAPpXhoI pool (pWAPpXhoI), BAC905 pool (BAC905) and swine genomic DNA digested by EcoRI during 4 h and hybridized by WAPpEcoRI-2.4 kb probe.

FIG. 4: Tissue specificity expression of the porcine wap transgene

Total RNA was prepared from various tissues of the different transgenic lines. Total RNA (10 μg) was added in each lane of a formaldehyde gel, transferred to a nylon membrane, and hybridized with a [³²P]-labeled porcine wap cDNA probe and a [³²P]-labeled murine wap cDNA probe. Hybridized material was visualized using X-rays films.

FIG. 5: Comparison of the level of the porcine wap mRNA in the mammary gland of 10-12-days lactating transgenic mice and of a 9-day lactating swine

Total RNA was prepared from mammary gland of a 10-day lactating non transgenic mouse (NT), 10 to 12 day of lactating transgenic animals, a virgin transgenic animal (S145) and a 9-day lactating swine. 10 μg of total RNA of the transgenic mice and 10, 5 and 1 μg of total RNA of the lactating non transgenic mouse and the lactating swine were added in each lane of a formaldehyde gel, transferred to a nylon membrane, and hybridized with a [³²P]-labeled porcine WAP cDNA probe (pig wap mRNA.), a [³²P]-labeled 18S rRNA probe (18S rRNA), and a [³²P]-labeled murine wap cDNA probe (mouse wap mRNA.). Hybridized material was visualized using X-rays films.

FIG. 6: Comparison of the porcine WAP protein concentration in the milk and in the whey of 10-12-days lactating transgenic mice and of 9-day lactating swine

Milk (0.1 μl) from a non transgenic mouse (NT), from transgenic mice (Bac16, Bac28, Bac29) and from a swine and swine whey (0.5 μl) (A.) or whey (0.05 μl) from a non transgenic mouse (NT), transgenic mice (Bac16, Bac28, Bac29) and swine whey (0.5 μl) (B.) were loaded on 16% SDS/PAGE and electrophoresed for 2 hours at 90V. Proteins were visualized by coomassie brillant blue coloration. Porcine WAP protein (pWAP) and murine WAP protein (mWAP) are indicated by arrows.

FIG. 7: Pig wap gene locus.

FIG. 8: The sequences of the page are SEQ ID No2 (assemble 19), SEQ ID No3 (assemble 17), SEQ ID No4 (assemble 20), SEQ ID No5 (assemble 12), SEQ ID No6 (assemble 18), SEQ ID No7 (assemble 21), and SEQ ID No8 (assemble 16). The complete sequence of the locus is therefore the continuation of SEQ ID No2 to SEQ ID No8.

EXAMPLE 1 Isolation and Characterization of Porcine wap Gene

Since the nucleic acid sequence of the porcine wap gene was unknown, the cloning of at least a part of the pig wap cDNA was necessary to isolate large genomic fragment from a BAC library. Thus, primers had to be designed in order to amplify specifically the porcine wap cDNA from the mammary gland of a lactating pig. The comparison of the mouse (Hennighausen and Sippel, 1982), rat (Campbell et al., 1984) and rabbit (Devinoy et al., 1988) WAP cDNA sequences showed that two regions are well conserved: the sequences of the signal peptide and the beginning of the third exon. Consequently, two primers were chosen in these conserved regions in order to amplify by RT-PCR the 5′end of the porcine wap cDNA. The unique band (220 bp) obtained by RT-PCR was isolated, cloned in pGEM-T vector (Promega) and both strand were sequenced. An examination of the three possible reading frames revealed that one of them showed a homology of 91.3% with the amino acid sequence of the porcine WAP published by Simpson et al., (1998). Two additional amino acids (aa₃₉ and aa₄₀) deduced from the sequence of the cloned DNA fragment were found in this part of the WAP protein. This difference between these two WAP protein sequences may result from errors in PCR or sequencing. Alternatively, it may reflect a polymorphism in the porcine wap gene.

From the sequence of the 5′ end of the porcine wap cDNA, two specific primers from the porcine wap gene were designed and the porcine BAC library was screened by PCR reaction with the two primer combinations. Five clones (283E5, 344H5, 829G1, 829G6, 905F9) containing the porcine wap gene were isolated and a restriction map was established (FIG. 1). The length of the genomic DNA fragment cloned in these BAC vectors ranged from 120 to 155 kb. Two clones appeared particularly interesting. The BAC 905F9 clone contained the wap gene in the middle of its insert and it then encompassed 70 kb upstream and 50 kb downstream the wap gene. The BAC 344H5 clone encompassed 130 kb upstream of the cap site of the wap gene. These two clones may contained some important elements for the regulation of the wap gene.

From this restriction map, we determined that a 5.4 kb XhoI fragment contained at least the 5′end wap gene. This XhoI fragment was cloned into the XhoI site of the plasmid vector Bluescrpit KS-. A primer walking strategy was chosen to sequence the two WAP gene DNA strands by the dideoxy method. The entire WAP gene was found in the 5.4 kb XhoI fragment and its sequence is available in the EMBL database under the accession number No AF320306.

The porcine wap gene extended over 2 kb. A putative TATA box was found at the expected position, ie −30 bp from the cap site. This TATA box did not look like a typical TATA consensus sequence (Breathnach and Chambon, 1981) but showed a modified sequence (TTTAAAA). Interestingly, this sequence was also found in the WAP gene of the other species (Devinoy et al., 1988) and in most of the milk protein genes studied so far. The pig wap gene was composed of four exons containing 109, 141, 160, 147 nucleotides respectively and three introns formed by 635, 327, 528 nucleotides. The first exon encoded the 28 nucleotides of the 5′-P untranslated region of the mRNA, the 19 amino acids of the signal peptide and the first 8 amino acids of the secreted WAP protein. The last exon included the last 4 amino acids and 129 nucleotides forming the 3′OH untranslated region.

Even if the structural organization of the wap gene was well conserved between species, a comparison of the sequence of the entire wap gene had revealed that only exon sequences were conserved. The sequence of introns showed a very low percentage of identity and their sizes were quite variable. For example, the third intron contained about 1.1 kb length in the mouse, approximately 500 bp in the rat, 369 bp in the rabbit and 517 bp in the pig. The amino acid sequence of the porcine wap showed a homology of 75, 50, 40 and 35% with the WAP proteins from camel, rabbit, rat and mouse respectively (Simpson et al., 1998). The porcine wap cDNA sequence showed a homology of 67.2, 61.6, 59.6% with wap cDNA from rabbit (Genbank:X07943), rat (Genbank:J00801) and mouse (Genbank:V00856) respectively.

EXAMPLE 2 Endogenous wap Gene Expression in Lactating Mammary Gland Materials and Methods

Twenty and ten μg of total RNA from the mammary gland of 5 days lactating swine, 3 days lactating rabbit and 3 days lactating mouse were separated by electrophoresis in three 1.5% agarose formaldehyde denaturing gels as previously described (Puissant et al., 1994). RNA was fragmented by treatment with 50 mM NaOH and then transferred by capillarity onto Biohylon-Z+ membrane (Bioprobe) in the presence of 50 mM sodium phosphate, pH 7. The mouse, rabbit and pig specific probes were obtained by PCR amplification with the degenerated wap1/wap4 primers using wap cDNA from rabbit, mouse and pig as template. The three probes were simultaneously labeled using the random priming technique (Sambrook et al., 1989). Hybridization was carried out overnight at 65° C., followed by autoradiography as previously described (Puissant et al., 1994).

Results:

The WAP protein was firstly isolated from the rodent milk and later in lagomorph, camel and pig milk. Its amount in the whey from different species is variable. Indeed, it was found at the concentration of 1 to 5 g/l in (McKenzie and Larson, 1978; Piletz et al., 1981; Hennighausen et al., 1990) versus 15 g/l in rabbit (Grabowski et al., 1991). Moreover, the production of endogenous WAP depends on the physiological state of the mammary gland since the level of the mouse wap mRNA increases several thousand-fold between the virgin state and mid lactation (Pittius et al., 1988a; Pittius et al., 1988b).

In order to know if the use of the cis-regulatory elements from the BAC clones encompassing the porcine wap gene may be interesting, it was necessary to determine if the level of the expression of the porcine wap gene was comparable to the expression level of the wap gene from rabbit and mouse. Total mammary RNA from five days lactating swine, three days lactating mouse and three days lactating rabbit were extracted and separated by electrophoresis. To obtain probes as similar as possible, three PCR amplifications were performed on RT products from mammary gland RNA with the same primers already used to clone pig wap cDNA and designed according to the conservation of the rabbit, mouse and rat wap cDNA. The three PCR products were purified and then simultaneously labeled with ³²P-dCTP by random priming technique in order to obtain specific activities as similar as possible. Hybridizations of the Northern blots were simultaneously carried out.

In the mammary gland of mouse, rabbit and swine, the wap mRNA was easily detectable (FIG. 2A, FIG. 2C and FIG. 2B respectively) since after only thirty minutes of autoradiography a signal was present. Each probe showed strictly species specific signal except for the porcine wap cDNA probe which partially cross-hybridized with the rabbit wap mRNA (FIG. 2B).

The UV/ethidium bromide picture (FIG. 2D) showed the equal loading of RNA. We may then compare the mRNA level of the different wap genes by quantification of the signals by phosphorimager. We found that the hybridization signal with the porcine wap mRNA was 5 to 8 fold lower and 6 to 8 fold lower than this observed with the mouse wap mRNA and the rabbit wap mRNA respectively.

EXAMPLE 3 Porcine wap Gene Expression in HC11 Cells Materials and Methods

The mouse mammary epithelial cell line HC11 was cultured in growth medium containing RPMI1640 (Eurobio), 10% heat-inactivated fetal bovine serum (FBS, Sigma), insulin (Life Technologies) 5 μg/ml and EGF (Life Technologies) 10 ng/ml as previously described (Ball et al., 1988). Cells were transfected by Lipofectamine® (Life Technologies) according to manufacturer's recommendations with 5 μg of plasmid or BAC DNA and 0,5 μg of the selection plasmid pRSVneo for one 6 cm diameter dish under 50% of confluence. Transfected cells were selected by adding 150 μg/ml of Geneticin in the growth medium. The pools of clones (at least 50 to 100 clones for each transfection) were cultured until confluence. After reaching the confluence, cells were cultured in the growth medium for 4 additional days followed by one day in the growth medium depleted of FBS and EGF but supplemented with transferrin and non essential amino acids (GC3-like medium). Milk protein gene expression was finally induced for the next two days by adding the lactogenic hormones to the GC3-like medium: Insulin (5 μg/ml), Dexamethasone (10⁻⁶M) and Prolactin (1 μg/ml).

Total RNA was prepared by RNAxel technique (Eurobio) according to the manufacturer's recommendations. RT-PCR analysis was carried out with the AMV reverse transcriptase (first strand cDNA synthesis kit for RT-PCR, Roche Diagnosys Boehringer Mannheim Corp., Indianapolis, USA) using 1 μg total RNA, the oligo(dT) primer and a combination of wap primers and of mouse GAPDH previously described (Lee et al., 1999).

The number of integrated copies was evaluated by Southern blot. 10 μg of genomic DNA were digested by EcoRI during 4 hours, fractionated on 1% agarose gel in TBE 1× and then blotted on Biohylon-Z+membrane (Bioprobe). Hybridization was performed with the labelled WAPpEcoRI 2,4 kb probe.

Results:

HC11 cell line is derived from the spontaneously immortalized COMMA ID cells which were isolated from the mammary gland of a midpregnant mouse (Ball et al., 1988). In this cell line, milk protein genes are sensitive to lactogenic hormones (insulin, hydrocortisone and prolactin) and to cell-cell interactions. Moreover, the transfected rat β-casein-cat gene expression was considerably enhanced under optimal conditions of induction previously defined (Doppler et al., 1990). In order to determine if the use of large genomic fragments of the porcine wap gene containing more regulatory elements allows a higher and better expression than smaller fragments, the comparison of the expression level of the porcine wap gene associated to only 1 kb of the promoter region (pWAPpXhoI) or associated to 70 kb upstream and 50 kb downstream of the porcine wap gene (BAC905F9) was performed. These two genomic fragments were transfected independently in HC11 cell line with a selection plasmid, pRSVneo. Pools of 50 to 100 clones were isolated by geneticin selection. Pools were maintained under confluence for four days in the complete culture medium and one more day in culture medium depleted in serum and EGF. Induction was then performed during two additional days with insulin, dexamethasone and prolactin. The level of expression in each pool was estimated by RT-PCR (FIG. 3).

The primers used for RT-PCR were specific of the porcine wap cDNA since no signal was obtained with the non transfected HC11 cells. The UV/ethidium bromide picture showed a higher amount of RT-PCR product with the RNA from BAC905F9 pool cells than from the pWAPpXhoI pool cells (FIG. 3A.). These RT-PCR products were transferred to nylon membrane and hybridized with the porcine wap cDNA probe. To normalize the RT-PCR amplification, the endogenous mouse GAPDH cDNA was amplified (FIG. 3C.) from the same RT sample by specific primers previously described (Lee et al., 1999). The quantification of the radioactive signal (FIG. 3B.) by the Phosporimager™ showed that the expression of the porcine wap gene was three times higher in cells transfected by the BAC905F9 clone than in cells transfected by the pWAPxhoI plasmid. Southern blot analysis (FIG. 3D.) revealed that 28 copies of the wap gene were integrated in the HC11 cell line genome in the case of cells transfected by the BAC 905F9 clone instead of 140 copies in the case of pWAPpXhoI transfection. Thus, the BAC clone allowed a fifteen fold higher expression per wap gene copy than a smaller genomic fragment.

EXAMPLE 4 Level of Expression in the Mammary Gland of Lactating Transgenic Mice

Materials and Methods

Isolation of the Porcine wap Gene BAC Insert for Micro-Injection and identification of Transgenic Animals

The isolation and characterization of the porcine wap gene BAC clones is reported in example 1 above. The BAC 344H5 clone was chosen for this study. BAC DNA prepared with the Nucleobond AX100 column from the Macherey-Naget kit was digested to completion with NotI and the DNA fragment used for the micro-injection of fertilized oocytes was prepared according to two different techniques. The first technique consisted in purifying the DNA fragments obtained after digesting the BAC by NotI by phenol-chloroform extraction. This fraction was directly microinjected into fertilized oocytes. In the second technique, the NotI DNA fragments were size-fractionated by field-inverted gel electrophoresis using a 1% low melting point agarose gel. The BAC insert containing the porcine wap gene was then isolated by GELase (Epicentre) and dialyzed as previously described (Schedl et al., 1993). The concentration of the purified DNA was estimated on a 1% agarose minigel. This BAC fragment, diluted at 1 to 5 ng/μl, was microinjected into the pronuclei of C57B16 X CBA fertilized oocytes. Transgenic mice were identified by PCR analysis performed on genomic DNA extracted from tails as previously described (Attal et al., 1995). Two specific primer sets were used. After 30 cycles of amplification, the PCR products were detected in 1% agarose gel.

Evaluation of Transgene Copy Number in Transgenic Mice by Southern Blot Analysis

In order to estimate the copy number of the transgene in each line, genomic DNA were extracted from tails after digestion by proteinase K (Roche) as previously described (Hogan et al., 1986). Genomic DNA (5 μg) from transgenic mice and from a swine was digested to completion with EcoRI restriction enzyme and size fractionated in 1% agarose gel overnight. The fragmented DNA was transferred onto nylon membrane (NytranN, Schleiher et shuell). The blot was hybridized with the labeled WAPpEcoRI 2.4 kb probe, shown in FIG. 1A. Signal quantification was done by autoradiography scanning using a Pharmacia LKB image-master DTS scanning system, according to the manufacturer's guidelines. The signal derived from the hybridization with porcine DNA serves to the two copies reference.

Expression of the Transgene

RNA was prepared by SV total RNA isolation system (Promega) according to the manufacturer's recommendations. Northern blot analysis was performed using 10 μg of the total RNA per sample and size fractionated in formaldehyde/agarose gel (Puissant et al., 1994). The fragmented RNA was transferred onto Biohylon-Z+ membrane (Qbiogene) and hybridized with the appropriate labeled probes. The hybridization signal obtained with the 18S rRNA probe (Raynal et al., 1984), was used as an internal standard to normalize the RNA loading between samples. The murine wap mRNA signal served as an internal standard to estimate differences of the endogenous gene transcription between animals.

Milk or whey protein were fractionated in 16% SDS/PAGE gel at 90V for 2 hours. Proteins were visualized a Coomassie brilliant blue R coloration.

Results

Generation of Transgenic Mice

Five BAC clones containing the porcine wap gene have been described above. When the pBeloBac11 vector was constructed, a NotI restriction site was introduced in its polylinker to separate easily the genomic fragments from the prokaryote DNA vector. Unfortunately, the five porcine wap gene BAC clones contained a NotI restriction enzyme site in their insert, located only 5 kb after the polyadenylation signal site of the porcine wap gene. Hence, it appeared difficult to use a long region downstream of the wap gene. We chose to generate transgenic mice with the BAC344H5 clone which contains the longest region upstream of the porcine wap gene (≈145 kb from the cap site).

Different techniques to extract DNA fragment from BAC clone useful for microinjection into fertilized oocytes have been described. Chrast and collaborators (1999) have tested three methods to extract DNA from 1% low melting point agarose gel. The first one consists in digesting agarose by agarase and purify DNA by a Qiagen tip100 column. The second method uses phenol-chloroform purification and ethanol precipitation instead of Qiagen column. The third method uses the electroelution from agarose. It was shown that the electroelution resulted in the best DNA yield and integrity. These techniques were tested to prepare the NotI fragment from the BAC344H5 clone. None of them gave DNA fragments utilizable for microinjection. For this reason, we chose to purify the insert of approximately 150 kb using two techniques. The first one did not involve the purification of the insert of interest from the two others since digested DNA was purified only by conventional phenol-chloroform extraction. The second technique involved the separation of the wap gene insert from the two others by size fractionation on 1% low melting point agarose gel and pulse field inverted electrophoresis The DNA was purified from agarose by GELase digestion following by a dialyze. These two preparations were microinjected into mouse eggs to produce transgenics.

Two transgenic animals (line 16 and 17) were identified by PCR analysis using genomic DNA from 21 born animals obtained with the DNA purified by phenol-chloroform. With the DNA prepared by the method using the GELase enzyme, 33 animals were born and six of them (line 24, 26, 28, 29, 30 and 107) were transgenics. The rate of transgenic animals was quite similar with one or the other DNA preparation. The animal BAC17 failed to transmit the transgene to its progeny. Nevertheless, 3 integrated copies were detected by Southern blot in this line. The animal BAC26 died before its reproduction and foreign DNA was not detectable by Southern blot. All other founders transmitted the transgene to their progeny and animals from the first generation were studied for transgene expression. The number of integrated copies was estimated by Southern analysis using EcoRI-digested genomic DNA from two or three mice per line. The probed used for hybridization was the 2.4 kb EcoRI fragment of porcine wap gene (FIG. 1A). Line 16 harbored 26 copies of the transgene, lines 24, 29, 30 had 1 copy, line 107 2 copies and line 28 3 copies.

Specificity of Transgene

Northern blot analysis using RNA from different tissues of transgenic animals from each lines showed that the porcine wap gene was expressed abundantly in the lactating mammary gland in all the transgenic lines (FIG. 4). The BAC vector containing the porcine wap gene thus prevented the extinction of the transgene frequently observed with gene constructs containing short genom DNA fragments. In all the six lines studied, the porcine wap mRNA was only detected in the mammary gland of lactating animals. No ectopic expression could be seen in the other examined tissues (liver, heart, kidney, duodenum, brain, salivary gland or stomach). Each Northern blot was hybridized with a mouse wap cDNA probe. The expression pattern of the porcine wap gene was compared to the endogenous wap gene expression. The expression of the porcine wap gene from the BAC344H5 clone integrated randomly in the mouse genome was as specifically expressed in the mammary gland as the mouse endogenous wap gene.

Level of Expression in the Mammary Gland of Lactating Transgenic Mice

In order to evaluate the level expression of the transgene in the mammary gland of the lactating transgenic animals and to compare it to the expression of the endogenous pig wap gene, total RNA from the mammary gland of a non transgenic lactating mouse, of transgenic lactating mice and of a lactating pig were analyzed by Northern blot (FIG. 5). Scale of total RNA loading (1, 5 or 10 μg) from mouse and pig were used to estimate more easily the level of specific mRNA. The first hybridization with a porcine wap cDNA probe showed that it did not cross-hybridized with the endogenous mouse wap mRNA since no signal was detected with the RNA from mammary gland of a non transgenic 10 day-lactating mouse. The data obtained from two or three transgenic animals per line revealed that the level of expression was quite different between the lines. The line 16 expressed abundantly the transgene whereas the five others showed similar expression level. One virgin female from the line 29 was also tested by Northern blotting. No porcine wap mRNA was found in the mammary gland of this animal. The same was true for the endogenous murine wap mRNA measured by a second hybridization with the mouse cDNA probe. The expression was therefore specific of the mammary gland of lactating animals.

The mouse wap cDNA probe was used as an internal standard to estimate the expression level of the endogenous milk protein gene. All animals showed a comparable mouse wap mRNA concentration except for the virgin animal (FIG. 5). The 18S rRNA probe was used as an internal standard to estimate the RNA loading in the gels. The level of expression of the porcine wap gene in the transgenic mice was compared to those of the endogenous porcine wap gene in a 9-day lactating swine. The ratio between the signals from the porcine wap cDNA probe hybridization and from the 18S rRNA probe hybridization were calculated. This ratio from the porcine mammary gland was arbitrary fixed to 1 and the other referred to it. Results are summarized in the table one. Only the line 16 had a content of porcine wap mRNA higher than a 9-day lactating swine. Two of three tested animals from the line 28 had porcine wap mRNA concentration similar to this observed in pig. The other animals showed a lower level of expression. The expression level varied slightly between animals from the same line, except for the line 28 and 107. Indeed, in one of the three studied animals from the line 28, the wap gene expression was nine 9 times lower expression than in two other animals. From the line 107, the animal named BAC183 showed a signal four times lower than the animal BAC181. In no case, different level of expression of endogenous murine wap gene could be seen.

TABLE 1 the wap gene expression level in the mammary gland of lactating transgenic mice Expression is the ratio between the porcine wap mRNA concentration in transgenic mice and the porcine wap mRNA concentration in a lactating swine. Copy numbers were estimated from Southern blot analyses carried out on two or three transgenic animals from each line. Porcine genomic DNA served as a 2 copies reference. Integrated Expression/2 Founders F1 animals Expression ratio copy number copies Bac 16 26 Bac 57 12.02 0.92 Bac 60 9.63 0.74 Bac 24 1 Bac89 0.36 0.72 Bac90 0.14 0.28 Bac 30 1 Bac103 0.37 0.74 Bac104 0.56 1.12 Bac 28 3 Bac123 0.22 0.14 Bac157 1.52 1.01 Bac170 1.92 1.28 Bac 29 1 Bac144 0.31 0.62 Bac148 0.23 0.46 Bac172 0.53 1.06 Bac 107 2 Bac181 0.58 0.58 Bac183 0.12 0.12

When the expression level was reported to the number of two integrated copies in transgenic mice, it appeared that it was quite similar to the level of expression of the pig wap gene in its natural genomic environment. Except for the two animals noted before (Bac123 and Bac183), the expression levels per 2 integrated copies related to the level of porcine wap gene expression varied not more than 1 to 3 fold between each animal. The expression of the transgene was therefore essentially correlated to the number of integrated copies.

To confirm the RNA analysis, the protein of the mouse milk were performed using denaturing polyacrylamide gel electrophoresis. Since no specific antibody anti pig WAP was available, the Coomassie brilliant blue R coloration was used to reveal the presence of each proteins in the mouse milk (FIG. 6). The porcine wap protein was displayed only in the milk or the whey from the animal Bac16. It is interesting to note that, in the same conditions, the endogenous WAP protein was not detected in the pig milk.

EXAMPLE 5 Further Characterization of the WAP Locus in Pig

The WAP locus in pig has been sequenced. Sequences of the invention are depicted as SEQ ID No2 (assemble 19), SEQ ID No3 (assemble 17), SEQ ID No4 (assemble 20), SEQ ID No5 (assemble 12), SEQ ID No6 (assemble 18), SEQ ID No7 (assemble 21), and SEQ ID No8 (assemble 16) (see FIGS. 7 and 8).

The complete sequence of the locus is therefore the continuation of SEQ ID No2 to SEQ ID No8. A gene having a strong homology with human RAMP3, encoding a transporter protein of a calcitonine-like receptor, has been found in this WAP locus.

In addition, transgenic mice containing the NotI fragment of BAC905F9 of about 80 Kb long and the AscI-NotI fragment of BAC344H5 of about 30 kb long have been obtained. We observed that the 80 Kb fragment allows high and specific expression of a transgene in the mammary gland of lactating transgenic mice.

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1. An isolated DNA molecule comprising the 5′ and 3′ regions of the pig whey acidic protein gene locus, wherein said DNA molecule is about 145 kb or 75 kb in length and is isolated from a NotI-NotI fragment of about 145 kb or 75 kb obtainable from BAC 905F9 or BAC 344H5 deposited at the Collection Nationale de Cultures de Micro-organismes (CNCM) under the accession numbers I-2595 and I-2596 respectively. 